Independent register of U.S. FDA drug recalls · updated Oct 12, 2026
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FDA Drug Recalls

14,806 recalls, newest first

Class II · Moderate risk

Gaviscon Liquid Antacid Extra Strength

Labeling: Label lacks warning - Magnesium safety warning is not present on the Gaviscon bottle label.

Terminated Labeling / mix-up Glaxosmithkline Consumer Healthcare Holdings NDC 0135-0095-41 D-1325-2020
Class II · Moderate risk

Lisinopril Tablets

Product Mix Up: Lisinopril 10 mg tablets were found in Lisinopril 5 mg 1000-count bottle.

Terminated Labeling / mix-up Lupin Pharmaceuticals Inc. NDC 68180-513-03 D-1290-2020
Class III · Low risk

Clonidine Hydrochloride Tablets

Failed Impurities/Degradation Specifications: potential migration of benzophenone at very low level into the product from container.

Terminated Impurity / degradation Unichem Pharmaceuticals USA INC NDC 29300-135-01 D-1291-2020
Class III · Low risk

Lamotrigine Tablets

Presence of Foreign Substance visually consistent with the silica granules present in the desiccant packs utilized during storage of the product.

Terminated Particulate / foreign matter Jubilant Cadista Pharmaceuticals, Inc. NDC 59746-247-97 D-1281-2020
Class II · Moderate risk

Doxycycline Hyclate Tablets

Failed Dissolution Specification: The dissolution test at the 24 month time point (end of shelf life) yielded an out-of-specification result.

Terminated Dissolution failure The Harvard Drug Group NDC 0904-0430-04 D-1288-2020
Class II · Moderate risk

Doxycycline Hyclate Tablets

Failed dissolution specification - dissolution results of 59% (spec. NLT 85%) at the 24 month time point (end of shelf life).

Terminated Dissolution failure American Health Packaging D-1293-2020
Class II · Moderate risk

EcoLips Sport Lip Balm

Superpotent Drug: The active ingredient, avobenzone, is used at 5% which is higher than the allowable 3% in the sunscreen formula per FDA sunscreen regulations.

Terminated Wrong potency / content Eco Lips Inc D-1310-2020
Class II · Moderate risk

Estriol USP Micronized 5 G

Failed impurities/ degradation specifications: Out of specification for organic impurities.

Terminated Impurity / degradation Triova Pharmaceuticals LLC NDC 71092-9977-02 D-1284-2020
Class III · Low risk

Gabapentin Tablets USP

Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.

Terminated Impurity / degradation InvaGen Pharmaceuticals, Inc. NDC 76282-405-05 D-1272-2020

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